Advances in our understanding of the molecular basis of disorders of platelet function von NURDEN, A., NURDEN, P.

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Inherited disorders of platelet function: selected updates von Nurden, A. T., Nurden, P.

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Inherited disorders of platelet function: selected updates von Nurden, A.T., Nurden, P.

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Recommendations for the standardization of light transmission aggregometry: a consensus of the working party from the platelet physiology subcommittee of SSC/ISTH von Cattaneo, M., Cerletti, C., Harrison, P., Hayward, C. P. M., Kenny, D., Nugent, D., Nurden, P., Rao, A. K., Schmaier, A. H., Watson, S. P., Lussana, F., Pugliano, M. T., Michelson, A. D.

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Autologous platelets as a source of proteins for healing and tissue regeneration von Anitua, Eduardo, Andia, Isabel, Ardanza, Bruno, Nurden, Paquita, Nurden, Alan T.

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Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders von Greinacher, A., Pecci, A., Kunishima, S., Althaus, K., Nurden, P., Balduini, C. L., Bakchoul, T.

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Autologous preparations rich in growth factors promote proliferation and induce VEGF and HGF production by human tendon cells in culture von Anitua, Eduardo, Andía, Isabel, Sanchez, Mikel, Azofra, Juan, Mar Zalduendo, M a del, la Fuente, María de, Nurden, Paquita, Nurden, Alan T.

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The abnormal proplatelet formation in MYH9‐related macrothrombocytopenia results from an increased actomyosin contractility and is rescued by myosin IIA inhibition von Chen, Y., Boukour, S., Milloud, R., Favier, R., Saposnik, B., Schlegel, N., Nurden, A., Raslova, H., Vainchenker, W., Balland, M., Nurden, P., Debili, N.

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Peripartum bleeding management in a patient with CalDAG‐GEFI deficiency von Canault, M., Saultier, P., Fauré, S., Poggi, M., Nurden, A. T, Nurden, P., Morange, P. E., Alessi, M‐C., Gris, J‐C.

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C560R[beta]3 caused platelet integrin [alpha]IIb[beta]3 to bind fibrinogen continuously, but resulted in a severe bleeding syndrome and increased murine mortality von Fang, J, Nurden, P, North, P, Nurden, A T, Du, L M, Valentin, N, Wilcox, D A

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Mean platelet volume: comparison of three analysers towards standardization of platelet morphological phenotype von LATGER-CANNARD, V., HOARAU, M., SALIGNAC, S., BAUMGART, D., NURDEN, P., LECOMPTE, T.

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Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients von FIORE, M., FIRAH, N., PILLOIS, X., NURDEN, P., HEILIG, R., NURDEN, A. T.

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Advantages of Fast-Acting ADP Receptor Blockade in Ischemic Heart Disease von Nurden, Alan T, Nurden, Paquita

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A Glanzmann thrombasthenia family associated with a TUBB1‐related macrothrombocytopenia von Guillet, Benoit, Bayart, Sophie, Pillois, Xavier, Nurden, Paquita, Caen, Jacques P., Nurden, Alan T.

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An acquired inhibitor to the GPVI platelet collagen receptor in a patient with lupus nephritis von NURDEN, P., TANDON, N., TAKIZAWA, H., COUZI, L., MOREL, D., FIORE, M., PILLOIS, X., LOYAU, S., JANDROT‐PERRUS, M., NURDEN, A. T.

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Clopidogrel: a review of its mechanism of action von Savi, P., Nurden, P., Nurden, A. T., Levy-Toledano, S., Herbert, J.-M.

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Altered megakaryocytopoiesis in von Willebrand type 2B disease von NURDEN, A. T., FEDERICI, A. B., NURDEN, P.

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C560Rβ3 caused platelet integrin αII b β3 to bind fibrinogen continuously, but resulted in a severe bleeding syndrome and increased murine mortality von Fang, J, Nurden, P, North, P, Nurden, A T, Du, L M, Valentin, N, Wilcox, D A

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Rebuttal: the French Gypsy mutation does not give rise to a particularly mild form of Glazmann's thrombasthenia von Nurden, A. T., Nurden, P.

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Mutation analysis for a patient with Glanzmann thrombasthenia who produced a landmark isoantibody to the αIIbβ3 integrin von NURDEN, A. T., KUNICKI, T., NURDEN, P., FIORE, M., MARTINS, N., HEILIG, R., PILLOIS, X.

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